Associated Papers
PCR-based detection of hereditary mutations in SLC2A9, BTBD17, and NECAP1 among native Korean dog breeds.
Kang M et al.
Journal of Veterinary Science, 2025
40765230 (PubMed )
Supplement: jvs-26-e48-s001.xls › Supplementary_Table_1
An Overview of Canine Inherited Neurological Disorders with Known Causal Variants.
Cocostîrc V et al.
Animals : an Open Access Journal From Mdpi, 2023
Neuronal ceroid lipofuscinosis in a German Shorthaired Pointer associated with a previously reported CLN8 nonsense variant.
Guo J et al.
Molecular Genetics and Metabolism Reports, 2019
Neuronal ceroid lipofuscinosis in Salukis is caused by a single base pair insertion in CLN8.
Lingaas F et al.
Animal Genetics, 2018
Canine neuronal ceroid lipofuscinoses: Promising models for preclinical testing of therapeutic interventions.
Katz ML et al.
Neurobiology of Disease, 2017
Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.
Hirz M et al.
Molecular Genetics and Metabolism, 2017
Homozygous PPT1 Splice Donor Mutation in a Cane Corso Dog With Neuronal Ceroid Lipofuscinosis.
Kolicheski A et al.
Journal of Veterinary Internal Medicine, 2017
Australian Cattle Dogs with Neuronal Ceroid Lipofuscinosis are Homozygous for a CLN5 Nonsense Mutation Previously Identified in Border Collies.
Kolicheski A et al.
Journal of Veterinary Internal Medicine, 2016
A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry.
Guo J et al.
Molecular Genetics and Metabolism, 2014
Golden Retriever dogs with neuronal ceroid lipofuscinosis have a two-base-pair deletion and frameshift in CLN5.
Gilliam D et al.
Molecular Genetics and Metabolism, 0
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